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J. Biol. Chem., Vol. 262, Issue 18, 8443-8446, Jun, 1987
PA Foster, CA Fulcher, T Marti, K Titani and TS Zimmerman
We have identified a Factor VIII (FVIII) binding domain residing within the
amino-terminal 272 amino acid residues of the mature von Willebrand Factor
(vWF) subunit. Two-dimensional crossed immunoelectrophoresis showed direct
binding of purified human FVIII to purified human vWF. After proteolytic
digestion of vWF with Staphylococcus aureus V8 protease (SP), FVIII binding
was seen only with the amino-terminal SP fragment III and not with the
carboxyl-terminal SP fragment II. A monoclonal anti-vWF antibody (C3)
partially blocked FVIII binding to vWF and SP fragment III. FVIII also
bound to vWF which had been adsorbed to polystyrene beads. This binding was
inhibited in a dose- dependent manner by whole vWF, SP fragment III, and by
monoclonal antibody C3. Binding could not be inhibited by SP fragment I,
which contains the middle portion of the vWF molecule, or by reduced and
alkylated whole vWF. SP fragment II caused only minimal inhibition. Trypsin
cleavage of SP fragment III produced a monomeric 35-kDa fragment containing
the amino-terminal 272 amino acid residues of vWF. This fragment reacted
with monoclonal antibody C3 and inhibited the binding of FVIII to vWF in a
dose-dependent manner. These studies demonstrate that a major FVIII binding
site resides within the amino- terminal 272 amino acid residues of vWF.
A major factor VIII binding domain resides within the amino-terminal 272 amino acid residues of von Willebrand factor
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